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RecruitingNCT07658326TendistressUpdated Jul 16, 2026

Preoperative Stress Assessment in Patients Undergoing Surgery for Rotator Cuff Tendinopathy

An observational study in Stress and Tendinopathy Rotator Cuff, sponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche. Recruiting at 3 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-16.

Sponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche · Observational

From the registry’s dates

  • Started Sep 2023; still recruiting 3 years later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

Orthopedic surgery of the limbs presents a unpredictable postoperative course, which can be more or less lengthy in terms of functional recovery and resumption of personal or professional activities. Not uncommon, convalescence can require many months with dramatic personal and/or socio-professional consequences (disability, unemployment, etc.), particularly in the postoperative development of complex regional pain syndrome (CRPS) and/or adhesive capsulitis.

Among the suspected contributing factors, the existence of an unfavorable preoperative psychological context in patients is often mentioned.

This research is based on the hypothesis that a high level of preoperative stress in patients could contribute to the occurrence of more significant postoperative complications in patients who have undergone shoulder surgery.

The main objective is to measure the level of preoperative stress in patients undergoing surgery for rotator cuff tendinopathy.

02

Conditions studied

  • Stress
  • Tendinopathy Rotator Cuff
03

In context

Lead sponsor

GCS Ramsay Santé pour l'Enseignement et la Recherche is the lead sponsor of 198 studies on the registry; 94 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients will be recruited from the orthopedic surgery department of the centers (Clinique de l'Union, Clinique la Croix du sud and Clinique des Cèdres).

Inclusion criteria

  • Patient, male or female, over 18 years of age
  • First-line surgery for rotator cuff tendinopathy (torn and untorn)
  • Subject affiliated with or covered by a social security scheme
  • Collection of the patient's non-opposition to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Patients with medical history of adhesive capsulitis or complex regional pain syndrome (CRPS)
  • Patients with a history of diabetes or thyroid dysfunction
  • Patients with a history of fibromyalgia
  • Patients with a history of mental illness (PMD, schizophrenia)
  • Patients taking antidepressants or similar medications
  • Patients participating in another clinical trial
  • Protected patients: adults under guardianship, curatorship, or other legal protection, deprived of liberty by judicial or administrative decision;
  • Pregnant, breastfeeding, or parturient women;
  • Patients hospitalized without their consent.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • patient undergoing surgery for rotator cuff tendinopathy

    Other: Questionnaires

Interventions

  • OtherQuestionnaires

    MSP9 score Cungi scale EVA scale

06

What researchers measure

Primary outcomes

  1. Stress will be assessed using the MSP9 score.

    This score ranges from 9 to 72 based on a rating scale of 1 to 8 (reversed for positive items): * 9-26 - Very low stress level * 27-44 - Low stress level * 45-54 - Moderate stress level * 55-63 - High stress level * 64-72 - Very high stress level

    Time frame: Preoperation

07

Study locations

3 of 3 sites recruiting
  • Clinique des Cèdres
    Cornebarrieu, 31700, France
    Recruiting
  • Clinique la croix du sud
    Quint-Fonsegrives, 31130, France
    Recruiting
  • Clinique de l'Union
    Saint-Jean, 31240, France
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07658326
Lead sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
Responsible party
Sponsor
First posted
Jun 22, 2026
Start date
Sep 28, 2023
Primary completion
Sep 2026 (estimated)
Completion
Sep 2026 (estimated)
Last update
Jul 16, 2026

Study contacts

Jean-François Oudet
Contact
jf.oudet@ecten.eu
0033683346567
Marie-Hélène Barba
Contact
mh.barba@ecten.eu

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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